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The protein encoded by FTSJ1 is a member of the S-adenosylmethionine-binding protein family. Additionally we are shipping FTSJ1 Proteins (2) and many more products for this protein.
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Human Polyclonal FTSJ1 Primary Antibody for EIA, WB - ABIN952395
Takano, Nakagawa, Inoue, Kamada, Kure, Goto: A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008
Show all 4 references for ABIN952395
we have provided strong evidence that human FTSJ1 is required for Cm32 and Gm34 modification of tRNAPhe.
A 50kb deletion at Xp11.23 including the two genes, SLC38A5 (show Slc38a5 Antibodies) and FTSJ1 was found in 3 brothers with moderate to severe mental retardation.
identified a novel FTSJ1 mutation in an X-linked mental retardation family through mutation screening of a cohort of 73 unrelated Japanese male probands with MR
Results suggest a positive association between genetic variants and nonsyndromic X-linked mental retardation in young male subjects in the Chinese Han population.
These findings suggest that genetic variations in FtsJ homolog 1 (E. coli) possibly influence human cognitive ability.
Spb1p is a homologous yeast nucleolar protein (show MCRS1 Antibodies)
The protein encoded by this gene is a member of the S-adenosylmethionine-binding protein family. It is a nucleolar protein and may be involved in the processing and modification of rRNA. Three alternatively spliced transcript variants encoding different isoforms have been described for this gene.
, 2'-O-ribose RNA methyltransferase TRM7 homolog
, cell division protein
, putative ribosomal RNA methyltransferase 1
, putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase
, rRNA (uridine-2'-O-)-methyltransferase
, tRNA methyltransferase 7 homolog
, FtsJ homolog 1
, FtsJ RNA methyltransferase homolog 1
, Ftsj homolog 1